Canonical Allele Identifier: CA518481459

Gene: ZDHHC9

Linked Data

• gnomAD v4: X-129823715-G-T
• COSMIC: COSM6303384 ; COSM6303385
• MyVariant Identifiers: chrX:g.128957691G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823715G>T , CM000685.2:g.129823715G>T	GRCh38
NC_000023.10:g.128957691G>T , CM000685.1:g.128957691G>T	GRCh37
NC_000023.9:g.128785372G>T	NCBI36
NG_021387.1:g.25220C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.451C>A MANE Select	ENSP00000349689.6:p.Arg151=
ENST00000357166.10:c.451C>A	ENSP00000349689.6:p.Arg151=
ENST00000371064.7:c.451C>A	ENSP00000360103.3:p.Arg151=
ENST00000406492.2:c.451C>A	ENSP00000383991.2:p.Arg151=
ENST00000433917.5:c.330C>A
ENST00000491039.1:n.74C>A
NM_001008222.2:c.451C>A	NP_001008223.1:p.Arg151=
NM_016032.3:c.451C>A	NP_057116.2:p.Arg151=
XM_011531347.1:c.451C>A	XP_011529649.1:p.Arg151=
XM_011531348.1:c.451C>A	XP_011529650.1:p.Arg151=
XM_011531348.3:c.451C>A	XP_011529650.1:p.Arg151=
XR_001755694.2:n.845C>A
NM_016032.4:c.451C>A MANE Select	NP_057116.2:p.Arg151=
NM_001008222.3:c.451C>A	NP_001008223.1:p.Arg151=